Heterociclos con nitrógeno (N)

Please enquire for more information about 3,4-Diamino-2,6-dichloropyridine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-Chloro-pyridazine-3-carboxylic acid ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride (DMCM) is a chiral organic solvent that is used as a reagent in organic synthesis. It can be prepared by reacting 2-chloro-3,4-dimethoxybenzaldehyde with methanol and hydrochloric acid. DMCM is used as an additive to acetonitrile to increase the specificity of reactions. It has been shown to produce the stereoselective oxidation of pantoprazole and sodium hydroxide solution at room temperature. DMCM has also been used in the synthesis of maltol using mass spectrometric analysis. This chemical can be purified by recrystallization from anhydrous hydroxide solution or by fractional distillation. Impurities in this compound are chloride, sulfoxide, and inorganic base.

Please enquire for more information about 1-(5-Methylpyridin-2-yl)ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Boc-4-ethynylpiperidine is a natural product that has been shown to bind to membranes and induce conformational changes in the membrane. This binding was mediated by a boronic ester group on the piperidine ring, which interacts with the hydrophobic membrane surface. The orientation of the molecule in relation to the membrane surface is determined by steric effects from its methyl groups. 1-Boc-4-ethynylpiperidine binds more tightly to undecane than to water, which may be due to its stronger hydrophobic interactions with the membrane surface. The functional theory of 1-Boc-4-ethynylpiperidine's mechanism of action is based on its ability to act as a nucleophile and react with a nucleophilic site on another molecule, such as an enzyme or membrane protein.

Please enquire for more information about 4-(1-Benzofuran-2-yl)pyrimidin-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-{[1-(tert-Butoxycarbonyl)piperidin-3-yl]methoxy}benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-Cyclopropyl-3-(piperidin-3-ylmethoxy)benzamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Used for antibody separation by hydrophobic charge induction chromatography

Please enquire for more information about 2-Methyl-5-(methylsulfonyl)pyrimidin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Cinnoline is a chemical compound that is structurally similar to phenol, containing a hydroxyl group, two nitrogen atoms and a cyclic structure. Cinnoline has been shown to have anti-inflammatory activity in rats with adjuvant-induced arthritis. The mechanism of the anti-inflammatory effect of cinnoline is not fully understood, but it may be due to its stability and ability to bind to biological molecules or its conformational properties. Cinnoline does not react with nitric acid, making it a good candidate for use in infectious diseases such as tuberculosis. It has also been shown to be stable in human serum and has low pharmacokinetic properties. The fluorescence intensity of cinnoline was found to increase when exposed to an electrochemical potential and can be used as a probe molecule for pharmacokinetics studies.

Please enquire for more information about 7-(Difluoromethyl)-5-methyl-4,5,6,7-tetrahydro[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

6,7-Dihydro-5H-1-pyridin-5-one is a pyridine that is an analogue of 2-ethylpyridine and catalyzes the reaction between benzylpyridines and oxidants. 6,7-Dihydro-5H-1-pyridin-5-one has been shown to be selective for the benzylpyridine moiety and can be used as a catalyst in the synthesis of benzylpyridines. This compound has been shown to produce high yields of benzylpyridines with high chemoselectivity.

Please enquire for more information about 4-Bromomethyl-4'-methyl-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-(Bromomethyl)-1-methylpiperidine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (R,S)-4-Boc-3-carboxymethyl-piperazin-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-Cyanopiperidine is a cyclohexane ring with a trifluoroacetic acid group. It is used in the synthesis of pharmaceutical preparations and has been shown to be stable in low-energy environments, such as when mixed with glycol ethers or chlorides. N-Cyanopiperidine is also used as an intermediate for the preparation of other compounds, such as metal carbonyl complexes and derivatives. N-Cyanopiperidine can be synthesized by reacting anhydrous hydrogen cyanide with piperidinium chloride in the presence of metal hydroxides. This reaction mechanism is known to produce two products: 1) a stable complex with a metal ion, and 2) a reaction product that contains the desired product and hydrogen cyanide.

Please enquire for more information about 1H-Imidazo[1,2-c]pyrrolo[2,3-e]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Stability N/A Applications (R)-(-)-4-Phenyl-2-oxazolidinone (cas# 90319-52-1) is a compound useful in organic synthesis.

Please enquire for more information about 1,3,6-Trimethyl-2-oxo-N-{3-[(E)-2-pyridin-4-ylvinyl]phenyl}-2,3-dihydro-1H-benzimidazole-5-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-Cbz-(R)-2-methylpiperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Acetamido-6-methylpyridine is a molecule that has the chemical formula C5H7N3O2. It is an anion with a negative charge of -1. In its solid state, it has a molecular weight of 146.11 g/mol and a diameter of 3.2 Å. The compound is soluble in water and has two amide groups that are responsible for the fluorescence of this molecule. 2-Acetamido-6-methylpyridine can be synthesized by reacting 4-amino-3-pyridinecarboxylic acid with chloride in water to form the corresponding oxime derivative, which reacts with ammonium acetate to form the desired product. This compound binds well to metal ions such as copper and zinc, meaning it can be used as a chelate ligand in mesoporous materials.

2-(2,6-Dioxo-piperidin-3-yl)-4-fluoroisoindoline-1,3-dione (2,6DPI) is a synthetic chemical compound that has been shown to inhibit NF-κB activation in vitro. 2,6DPI is a competitive inhibitor of the p65 subunit of NF-κB and functions by binding to the cysteine residue on the p65 subunit. It has been shown to be effective against inflammatory diseases such as pulmonary disease and inflammation. This drug also inhibits deacetylases, which are enzymes involved in regulating gene expression. 2,6DPI may have therapeutic potential for the treatment of inflammatory diseases and cancer.

Applications 1-ACETYL-2-PIPERIDINEACETIC ACID (cas# 25393-20-8) is a useful research chemical.

2-Chloro-5-fluoro-4-(methylsulfanyl)pyrimidine is a drug that inhibits the activity of protein kinases. It has been shown to be an inhibitor of the enzyme protein kinase, which is involved in the process of inflammation, and also has been shown to have inhibitory effects on cytochrome P450 3A4 (CYP3A4) and p-glycoprotein. 2-Chloro-5-fluoro-4-(methylsulfanyl)pyrimidine has been shown to be effective against rheumatoid arthritis by inhibiting the production of inflammatory cytokines.

Please enquire for more information about 5-Chloro-3-iodo-1H-pyrazolo[4,3-b]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Cyanopyridine is an organic compound with the chemical formula (CN)N. It is a white solid that is soluble in water and polar solvents. When exposed to hydrochloric acid, 4-cyanopyridine undergoes a reaction that converts it to picolinic acid. This reaction proceeds through a mechanism in which the nucleophilic hydroxyl group of 4-cyanopyridine attacks the protonated nitrogen atom of hydrochloric acid. The resulting intermediate then loses a proton and becomes picolinic acid. Kinetic data on this reaction has been obtained from UV-vis spectroscopy, X-ray diffraction, and mass spectrometry experiments. The crystal structures of the bound form of 4-cyanopyridine and its quinoline derivatives have also been determined by x-ray crystallography.

Applications 1-(1-Oxidobenzo[d]isothiazol-3-yl)piperazine 1-Oxide Hydrochloride is an intermediate in the synthesis of Ziprasidone (Z485010) related compounds. References Huang, M., et al.: Clin. Pharmacol. Ther., 54, 257 (1993), Prakash, C., et al.: Drug Metab. Dispos., 25, 206 (1997), Brosen, K., et al.: Eur. J. Clin. Pharmacol., 44, 349 (1993),

Isoxazolo[4,5-b]pyrazin-3-amine is a chromatographic, efficient and scalable process for the synthesis of nitrogen heterocycles in a high yielding operationally simple chemistry. The reaction solvent can be easily removed by vacuum distillation, which makes it an ideal operationally simple and scalable process. The reaction can be conducted with various functionalized reagents to give a range of products. Isoxazolo[4,5-b]pyrazin-3-amine has been used in the synthesis of pharmaceutically important compounds such as antibiotics, antihistamines and anticancer agents.